A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263524



Internal ID20472742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26368856..26368985hg38UCSC Ensembl
chr8:26226372..26226501hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736862
Supporting Variants
Samples
Known GenesPPP2R2A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263524
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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